Kim Byung Hak, Hong Seong Su, Kwon Soon Woo, Lee Hwa Young, Sung Hyeran, Lee In-Jeong, Hwang Bang Yeon, Song Sukgil, Lee Chong-Kil, Chung Daehyun, Ahn Byeongwoo, Nam Sang-Yoon, Han Sang-Bae, Kim Youngsoo
College of Pharmacy, Chungbuk National University, Cheongju, Korea.
J Pharmacol Exp Ther. 2008 Nov;327(2):393-401. doi: 10.1124/jpet.108.140145. Epub 2008 Aug 11.
Diarctigenin was previously isolated as an inhibitor of nitric oxide (NO) production in macrophages from the seeds of Arctium lappa used as an alternative medicine for the treatment of inflammatory disorders. However, little is known about the molecular basis of these effects. Here, we demonstrated that diarctigenin inhibited the production of NO, prostaglandin E(2), tumor necrosis factor-alpha, and interleukin (IL)-1beta and IL-6 with IC(50) values of 6 to 12 miciroM in zymosan- or lipopolysaccharide-(LPS) activated macrophages. Diarctigenin attenuated zymosan-induced mRNA synthesis of inducible NO synthase (iNOS) and also inhibited promoter activities of iNOS and cytokine genes in the cells. Because nuclear factor (NF)-kappaB plays a pivotal role in inflammatory gene transcription, we next investigated the effect of diarctigenin on NF-kappaB activation. Diarctigenin inhibited the transcriptional activity and DNA binding ability of NF-kappaB in zymosan-activated macrophages but did not affect the degradation and phosphorylation of inhibitory kappaB (IkappaB) proteins. Moreover, diarctigenin suppressed expression vector NF-kappaB p65-elicited NF-kappaB activation and also iNOS promoter activity, indicating that the compound could directly target an NF-kappa-activating signal cascade downstream of IkappaB degradation and inhibit NF-kappaB-regulated iNOS expression. Diarctigenin also inhibited the in vitro DNA binding ability of NF-kappaB but did not affect the nuclear import of NF-kappaB p65 in the cells. Taken together, diarctigenin down-regulated zymosan- or LPS-induced inflammatory gene transcription in macrophages, which was due to direct inhibition of the DNA binding ability of NF-kappaB. Finally, this study provides a pharmacological potential of diarctigenin in the NF-kappaB-associated inflammatory disorders.
牛蒡子苷元先前是从牛蒡种子中分离出来的一种巨噬细胞中一氧化氮(NO)产生的抑制剂,牛蒡种子被用作治疗炎症性疾病的替代药物。然而,对于这些作用的分子基础知之甚少。在此,我们证明牛蒡子苷元在酵母聚糖或脂多糖(LPS)激活的巨噬细胞中抑制NO、前列腺素E2、肿瘤坏死因子-α以及白细胞介素(IL)-1β和IL-6的产生,其IC50值为6至12微摩尔。牛蒡子苷元减弱酵母聚糖诱导的诱导型一氧化氮合酶(iNOS)的mRNA合成,并且还抑制细胞中iNOS和细胞因子基因的启动子活性。由于核因子(NF)-κB在炎症基因转录中起关键作用,接下来我们研究了牛蒡子苷元对NF-κB激活的影响。牛蒡子苷元抑制酵母聚糖激活的巨噬细胞中NF-κB的转录活性和DNA结合能力,但不影响抑制性κB(IkappaB)蛋白的降解和磷酸化。此外,牛蒡子苷元抑制表达载体NF-κB p65引发的NF-κB激活以及iNOS启动子活性,表明该化合物可直接靶向IkappaB降解下游的NF-κB激活信号级联并抑制NF-κB调节的iNOS表达。牛蒡子苷元还抑制NF-κB的体外DNA结合能力,但不影响细胞中NF-κB p65的核转运。综上所述,牛蒡子苷元下调酵母聚糖或LPS诱导的巨噬细胞炎症基因转录,这是由于直接抑制NF-κB的DNA结合能力。最后,本研究揭示了牛蒡子苷元在NF-κB相关炎症性疾病中的药理学潜力。